Laboratory Methods Cell Cycle Lengths Generation time (hrs) Days needed for 26 generations (colony) E. coli 0.33 0.36 Nancy Connell, PhD Professor, nfectious Disease Department of Medicine Center for Emerging Pathogens UMDNJ-NJ Medical School TB Program Managers Workshop 2009 M. smegmatis 2.5 2.7 M. tuberculosis 22.0 24.0 Mycobacterial cell wall Mycobacteria have a cell envelope with a high lipid content This characteristic accounts for the difficulty in staining them with conventional techniques. Mycobacteria have N-glycolylmuramic acid in the place of N-acetyl muramic acid in their peptidoglycan (cell wall) Outline of Laboratory Methods 1. Processing 2. Staining 3. Growth characteristics 4. Susceptibility testing 5. Safety in the laboratory http://www.scielo.br/img/revistas/mioc/v101n7/v101n7a01f01.gif
Laboratory Principles Digestion / Decontamination (non-sterile specimen types) Concentration Smear Exam Culture Susceptibility Molecular techniques (PCR, genotyping) Digestion/Decontamination Traditional method: 4% NaOH Decontamination: time of exposure must be carefully controlled Most common method: N-acetyl-L-cysteine (NALC) + 2% NaOH - mild decontamination solution (NaOH) with mucolytic agent (NALC) to free trapped mycobacteria from mucus 4% Sulfuric acid Often used for decontaminating urine specimens 5% Oxalic acid Most useful for processing specimens that contain Pseudomonas aeruginosa as a contaminant Smear - Stains Acid-fastness (mycolic acids) Cannot be decolorized with acid alcohol Stains: Ziehl-Neelsen - carbolfuchsin hot stain Kinyoun - carbolfuchsin cold stain Higher concentration of phenol instead of heat Auramine Fluorochrome stain Most sensitive Mycobacteria tuberculosis Ziehl-Neelsen Stain Mycobacterium tuberculosis is a slim (1-4µm), unencapsulated, strongly acid-fast rod that frequently shows irregular beading due to vacuoles and polyphosphate granules.
Mycobacteria tuberculosis Auramine Stain AFB Smear nterpretation Fluorochrome (read minimum of 30 fields[f]-about 2 mins) AFB Seen (40X) Report 0 No AFB 1-2 / 70F (1.5 sweeps) Doubtful 2-18 / 50F (1 sweep) Rare (1+) AFB 4-36 / 10F Few (2+) AFB 4-36 / F Moderate (3+) AFB >36 / F Numerous (4+) AFB AFB Smear nterpretation Kinyoun - Specimen (read approximately 300 fields[f] - 15 mins) AFB Seen (100X) Report 0 No AFB 1-2 / 300F (3 sweeps) Doubtful 1-9 / 100F Rare (1+) AFB 1-9 / 10F Few (2+) AFB 1-9 / F Moderate (3+) AFB >9 / F Numerous (4+) AFB Growth Requirements One of the least fastidious of pathogenic microorganisms Aerobes, prefer 5% to 10% CO 2 for primary recovery Microaerophilic metabolism during latent infection Recent drug/vaccine development focuses on this characteristic Multiply slowly, dividing only every 18-24 hours Serpentine growth, cord factor- 6,6- dimycolytrehalose Cord factor is virulence factor
Cording Caused by 6,6-dimycolytrehalose ( cord factor ) Culture Media Four traditional culture media: Egg-based (Lowenstein Jensen) Agar-based (Middlebrook agar) Liquid (Middlebrook broth) Selective media (susceptibility assays) TB is a slow growing, rough, buff colony on solid media Lowenstein Jensen MGT Media M. tuberculosis - Crumbly buff colored colonies
dentification Traditional - biochemicals (indirect) Niacin positive, nitrate negative solate from solid media required, test takes days to weeks Rapid Direct - Nucleic Acid Amplification Can be performed within hours of specimen receipt DNA probe of isolate Can be performed in hours on pellet from rapid broth culture Commercially available probes: M. tuberculosis, M. avium-intracellulare, M. kansasii, M. gordonae Drug Resistance and Susceptibility Testing Anti-tuberculosis Drugs Drug-resistant TB First-Line Drugs soniazid Rifampin Pyrazinamide Ethambutol Rifabutin* Rifapentine Second-Line Drugs Cycloserine P-Aminosalicylic acid Ethionamide Amikacinor kanamycin* Levifloxacin* Moxifloxacin* MDR-TB: resistant to at least isoniazid and rifampin XDR-TB: resistant to isoniazid and rifampin plus resistant to any fluoroquinolone and at least one of three injectable second-line drugs (i.e., amikacin, kanamycin, or capreomycin) *Not approved by the US Food and Drug Administration for the treatment of TB
Evolution of Drug Resistance - 1 NH RF PZA Evolution of Drug Resistance - 2 P R R P NH NH RF R R R R R R R R PR R R R Susceptible TB Drug resistant M. tuberculosis MDR-TB XDR-TB TDR-TB
Susceptibility Testing Direct Performed directly from specimens with positive smears More accurate than indirect, faster turnaround ndirect Performed on recovered isolate Resistant isolates often grow more slowly, and are overgrown by more sensitive isolates Susceptibility Testing - 1 Proportional method most common method >1% growth represents resistance Susceptibility Testing - 2 TB Turn Around Times Bactec method Uses liquid media, faster than proportional method 90% to 100% agreement with proportional method Media contains 14 C-fatty acids: bacteria release 14 C- CO 2, which is detected AFB smear: Growth detection: TB identification: Susceptibility testing: 24 hours 14 days 21 days 28-30 days
False Negatives nfection with low numbers of organisms common Too small a sample could miss organisms Sputum 10 ml No swabs from wounds - tissue biopsies Urine (1 st morning total void) Large volume of pleural fluid dilutes out the few numbers of organisms (as much as possible of sample should be collected and processed) Too few specimens At least 3 sputums 3-5 urines Wrong site False Positives M. tuberculosis very hardy & survives well under very harsh conditions Cross Contamination possible from: Other positive specimens Quality control isolates Common scenario Specimen with 3+ or 4+ smear processed at same time as questionable patient specimen Patient has multiple specimens, none have positive smear and only one culture grows DNA fingerprinting can be helpful to determine possible cross contamination How can tell if am being exposed to a hazardous substance? Biosafety in the TB Laboratory Know what you are working with Ask questions Look at the container labeling Review the Material Safety Data Sheet Call Safety Officers
Use Your Senses What are we protecting against? Odors Eye rritations Visible Clouds or Fumes Spills Look for leaking containers, dripping liquid, puddles, etc. Ways to minimize exposure - 1 1. Substitution: Use of a less hazardous or attenuated material to reduce or eliminate hazard 2. Engineering Controls: Use of available technology and devices to isolate hazards from the worker 3. Administrative Controls: Monitor compliance, provide accessibility of control methods, investigate exposures to prevent future occurrence Ways to minimize exposure - 2 4. Work Practice Controls: Manner in which task is performed to reduce exposure: -Wash hands after removal of gloves -Disposal of needles without recapping -No lab coats outside of lab 5. PPE: Personal protective equipment: Specialized clothing or equipment used to protect workers from exposure: lab coats, gloves, face shields, eye protection, fluid resistant aprons, head and foot covering
Exposure ncident A specific incident of contact with potentially infectious material, body fluid, or chemical Procedures Following an Exposure mmediately wash affected area(s) Recover & save the specimen; refrigerate if possible Notify your supervisor Report all accidents involving body fluids or chemicals Getting treatment within a few hours of injury reduces the chance of sero-converting to HV Summary The TB lab works hard with a difficult organism TB laboratory diagnosis and treatment is extremely challenging: TB bacteria are notoriously slow-growing and culture takes time Molecular methods are under development but are not yet reliable Culture remains the gold standard of identification and susceptibility testing